Variant report

Variant	esv2761467
Chromosome Location	chr8:126368375-126385095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:205)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:205 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:126374993-126375347	K562	blood:	n/a	n/a
2	ATF2	chr8:126374985-126375397	GM12878	blood:	n/a	n/a
3	ATF2	chr8:126374854-126375451	GM12878	blood:	n/a	n/a
4	ATF3	chr8:126374920-126375429	A549	lung:	n/a	chr8:126375161-126375176
5	ATF3	chr8:126374854-126375624	HCT-116	colon:	n/a	chr8:126375161-126375176
6	ATF3	chr8:126375014-126375360	K562	blood:	n/a	chr8:126375161-126375176
7	BCL3	chr8:126383486-126384202	A549	lung:	n/a	n/a
8	BHLHE40	chr8:126375035-126375326	K562	blood:	n/a	n/a
9	BRCA1	chr8:126369442-126369463	GM12878	blood:	n/a	n/a
10	CBX3	chr8:126381909-126382119	K562	blood:	n/a	n/a
11	CBX3	chr8:126381888-126382290	K562	blood:	n/a	n/a
12	CBX3	chr8:126374962-126375414	K562	blood:	n/a	n/a
13	CEBPB	chr8:126384100-126384373	HepG2	liver:	n/a	chr8:126384261-126384272
14	CEBPB	chr8:126383715-126384422	A549	lung:	n/a	chr8:126384261-126384272
15	CEBPB	chr8:126383627-126384421	Hela-S3	cervix:	n/a	chr8:126384261-126384272
16	CEBPB	chr8:126384067-126384520	ECC-1	luminal epithelium:	n/a	chr8:126384261-126384272
17	CEBPB	chr8:126383625-126384616	MCF-7	breast:	n/a	chr8:126384261-126384272
18	CEBPB	chr8:126383710-126383938	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:126383862-126384640	HCT-116	colon:	n/a	chr8:126384261-126384272
20	CEBPB	chr8:126384193-126384405	HepG2	liver:	n/a	chr8:126384261-126384272
21	CEBPB	chr8:126383699-126384746	HCT-116	colon:	n/a	chr8:126384261-126384272
22	CEBPB	chr8:126383258-126384830	A549	lung:	n/a	chr8:126384261-126384272
23	CEBPB	chr8:126383563-126384528	A549	lung:	n/a	chr8:126384261-126384272
24	CEBPB	chr8:126374251-126374565	IMR90	lung:	n/a	n/a
25	CEBPB	chr8:126384017-126384537	MCF-7	breast:	n/a	chr8:126384261-126384272
26	CEBPB	chr8:126384161-126384417	IMR90	lung:	n/a	chr8:126384261-126384272
27	CEBPB	chr8:126374984-126375251	IMR90	lung:	n/a	chr8:126375108-126375120
28	CEBPB	chr8:126384153-126384412	H1-hESC	embryonic stem cell:	n/a	chr8:126384261-126384272
29	CEBPB	chr8:126383983-126384530	ECC-1	luminal epithelium:	n/a	chr8:126384261-126384272
30	CEBPB	chr8:126384141-126384356	HepG2	liver:	n/a	chr8:126384261-126384272
31	CHD1	chr8:126373671-126375692	IMR90	lung:	n/a	n/a
32	CHD1	chr8:126372837-126373439	IMR90	lung:	n/a	n/a
33	CHD2	chr8:126383053-126383249	K562	blood:	n/a	n/a
34	CREB1	chr8:126374942-126375409	K562	blood:	n/a	chr8:126375162-126375175
35	CREB1	chr8:126374868-126375476	GM12878	blood:	n/a	chr8:126375162-126375175
36	CREB1	chr8:126374928-126375496	GM12878	blood:	n/a	chr8:126375162-126375175
37	CTCF	chr8:126369720-126369870	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:126369620-126369770	K562	blood:	n/a	n/a
39	CTCF	chr8:126369700-126369850	BE2_C	brain:	n/a	n/a
40	CTCF	chr8:126369700-126369850	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:126369700-126369850	HCT-116	colon:	n/a	n/a
42	CTCF	chr8:126369660-126369810	K562	blood:	n/a	n/a
43	CTCF	chr8:126369660-126369810	GM12875	blood:	n/a	n/a
44	CTCF	chr8:126377500-126377650	A549	lung:	n/a	n/a
45	CTCF	chr8:126369680-126369830	A549	lung:	n/a	n/a
46	CTCF	chr8:126369700-126369850	HEK293	kidney:	n/a	n/a
47	CTCF	chr8:126369580-126369730	Caco-2	colon:	n/a	n/a
48	CTCF	chr8:126369660-126369810	HepG2	liver:	n/a	n/a
49	CTCF	chr8:126369660-126369810	GM12873	blood:	n/a	n/a
50	CTCF	chr8:126369640-126369790	GM12873	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:126374251-126374301	HRPEpiC	eye:	n/a
2	chr8:126384593-126384643	HRCEpiC	kidney:	n/a
3	chr8:126384593-126384643	NHDF-neo	bronchial:	n/a
4	chr8:126374251-126374301	PANC-1	pancreas:	n/a
5	chr8:126384593-126384643	GM06990	blood:	n/a
6	chr8:126374251-126374301	GM12892	blood:	n/a
7	chr8:126384593-126384643	HCT-116	colon:	n/a
8	chr8:126384593-126384643	ProgFib	skin:	n/a
9	chr8:126384593-126384643	HCF	heart:	n/a
10	chr8:126384593-126384643	HEEpiC	esophagus:	n/a
11	chr8:126374251-126374301	SAEC	small airway:	n/a
12	chr8:126384593-126384643	U87	brain:	n/a
13	chr8:126374251-126374301	HCT-116	colon:	n/a
14	chr8:126374251-126374301	AG09319	gingival:	n/a
15	chr8:126374251-126374301	HEEpiC	esophagus:	n/a
16	chr8:126374251-126374301	LNCaP	prostate:	n/a
17	chr8:126384593-126384643	HIPEpiC	eye:	n/a
18	chr8:126374251-126374301	NHBE	bronchial:	n/a
19	chr8:126384593-126384643	GM12892	blood:	n/a
20	chr8:126384593-126384643	HepG2	liver:	n/a
21	chr8:126384593-126384643	PFSK-1	brain:	n/a
22	chr8:126384593-126384643	Hela-S3	cervix:	n/a
23	chr8:126374251-126374301	NHDF-neo	bronchial:	n/a
24	chr8:126384593-126384643	HMEC	breast:	n/a
25	chr8:126384593-126384643	CMK	blood:	n/a
26	chr8:126384593-126384643	HNPCEpiC	eye:	n/a
27	chr8:126374251-126374301	SKMC	muscle:	n/a
28	chr8:126384593-126384643	HCM	heart:	n/a
29	chr8:126384593-126384643	HUVEC	blood vessel:	n/a
30	chr8:126374251-126374301	HMEC	breast:	n/a
31	chr8:126384593-126384643	Caco-2	colon:	n/a
32	chr8:126384593-126384643	NB4	blood:	n/a
33	chr8:126374251-126374301	NB4	blood:	n/a
34	chr8:126384593-126384643	HRE	kidney:	n/a
35	chr8:126374251-126374301	ProgFib	skin:	n/a
36	chr8:126374251-126374301	K562	blood:	n/a
37	chr8:126384593-126384643	T-47D	breast:	n/a
38	chr8:126374251-126374301	H1-hESC	embryonic stem cell:	embryo
39	chr8:126384593-126384643	HL-60	blood:	n/a
40	chr8:126384593-126384643	AoSMC	blood vessel:	n/a
41	chr8:126374251-126374301	HCM	heart:	n/a
42	chr8:126374251-126374301	PFSK-1	brain:	n/a
43	chr8:126374251-126374301	HCPEpiC	choroid plexus:	n/a
44	chr8:126374251-126374301	SK-N-MC	brain:	n/a
45	chr8:126374251-126374301	GM06990	blood:	n/a
46	chr8:126374251-126374301	T-47D	breast:	n/a
47	chr8:126374251-126374301	MCF10A-Er-Src	breast:	n/a
48	chr8:126374251-126374301	HRE	kidney:	n/a
49	chr8:126374251-126374301	U87	brain:	n/a
50	chr8:126374251-126374301	HCF	heart:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:126375605..126377607-chr8:126380197..126382660,2	K562	blood:
2	chr8:126362447..126364005-chr8:126367534..126370011,2	MCF-7	breast:
3	chr8:126366805..126369282-chr8:126440468..126443244,2	K562	blood:
4	chr8:126373175..126375171-chr8:126442465..126444112,2	K562	blood:
5	chr8:126367782..126370387-chr8:126440468..126442210,2	K562	blood:
6	chr8:126383732..126385634-chr8:126386782..126388926,2	MCF-7	breast:
7	chr8:126378716..126380659-chr8:126383858..126387902,3	K562	blood:
8	chr8:126379101..126380902-chr8:126383858..126386821,2	K562	blood:
9	chr8:126371278..126373915-chr8:126440851..126442526,2	MCF-7	breast:
10	chr8:126373622..126375800-chr8:126376213..126378817,2	MCF-7	breast:
11	chr8:126378716..126380659-chr8:126383858..126387902,3	K562	blood:
12	chr8:126379863..126381491-chr8:126392871..126395195,2	MCF-7	breast:
13	chr8:126376867..126379687-chr8:126439700..126442578,3	MCF-7	breast:
14	chr8:126377962..126381819-chr8:126440507..126443718,4	MCF-7	breast:
15	chr8:126374530..126376049-chr8:126380618..126383134,2	K562	blood:
16	chr8:126379101..126380902-chr8:126383858..126386821,2	K562	blood:
17	chr8:126375605..126377607-chr8:126380197..126382660,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254431	TF binding region
NSMCE2	TF binding region
ENSG00000254431	CpG island
NSMCE2	CpG island
ENSG00000173334	chromatin interactions
ENSG00000156831	chromatin interactions
ENSG00000254431	chromatin interactions

Extended variants
information (count: 649 )
Associated
traits (count: 148 )

Variant overlapped rSNPs/rCNVs (count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7822592	chr8:126368375-126368376	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190317012	chr8:126368389-126368390	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs565936906	chr8:126368465-126368466	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs551495045	chr8:126368468-126368469	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs536062585	chr8:126368478-126368479	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571116321	chr8:126368480-126368481	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577446840	chr8:126368482-126368483	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs533785787	chr8:126368485-126368486	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs140283424	chr8:126368486-126368487	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553753020	chr8:126368500-126368501	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs114208587	chr8:126368532-126368533	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs36020150	chr8:126368569-126368570	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536173049	chr8:126368570-126368571	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533091116	chr8:126368575-126368576	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs75174580	chr8:126368587-126368588	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369622865	chr8:126368590-126368591	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs555915823	chr8:126368593-126368594	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs370728280	chr8:126368608-126368609	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs575876952	chr8:126368658-126368659	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs544293129	chr8:126368670-126368671	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs181513197	chr8:126368674-126368675	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577913533	chr8:126368695-126368696	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs186580672	chr8:126368700-126368701	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs190058897	chr8:126368762-126368763	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs529597234	chr8:126368805-126368806	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145712796	chr8:126368815-126368816	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563063620	chr8:126368858-126368859	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs569309846	chr8:126368946-126368947	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531950491	chr8:126368948-126368949	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs181267803	chr8:126369007-126369008	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73338860	chr8:126369035-126369036	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs533519022	chr8:126369071-126369072	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs2385095	chr8:126369112-126369113	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs112742490	chr8:126369175-126369176	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs547351151	chr8:126369180-126369181	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs4242368	chr8:126369240-126369241	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs201908064	chr8:126369250-126369251	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs567057847	chr8:126369273-126369274	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536135835	chr8:126369278-126369279	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs73338863	chr8:126369300-126369301	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185468692	chr8:126369330-126369331	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535200797	chr8:126369333-126369334	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538832902	chr8:126369352-126369353	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs557945364	chr8:126369373-126369374	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377230348	chr8:126369415-126369416	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374119758	chr8:126369419-126369420	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368303019	chr8:126369420-126369421	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs201826786	chr8:126369434-126369435	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs372016316	chr8:126369443-126369444	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189778545	chr8:126369447-126369448	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:148)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Ovarian cancer	21240255	CNVD
Glioma	20126413	CNVD
Gastric cancer	21635755	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126322000-126374200	Weak transcription	Aorta	Aorta
2	chr8:126330800-126369200	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr8:126332600-126369400	Weak transcription	Fetal Stomach	stomach
4	chr8:126342000-126369400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr8:126348800-126369800	Weak transcription	Gastric	stomach
6	chr8:126353200-126369600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr8:126354000-126381200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr8:126354800-126369000	Weak transcription	Ovary	ovary
9	chr8:126354800-126371800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:126354800-126379800	Weak transcription	Pancreas	Pancrea
11	chr8:126354800-126380400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr8:126354800-126381600	Weak transcription	Brain Anterior Caudate	brain
13	chr8:126354800-126383200	Weak transcription	Brain Angular Gyrus	brain
14	chr8:126355000-126369400	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr8:126355000-126369600	Weak transcription	Fetal Intestine Large	intestine
16	chr8:126355000-126374600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:126355200-126369400	Weak transcription	Left Ventricle	heart
18	chr8:126355200-126369400	Weak transcription	Spleen	Spleen
19	chr8:126355200-126369400	Weak transcription	K562	blood
20	chr8:126355200-126369800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr8:126355200-126373000	Weak transcription	NH-A	brain
22	chr8:126355200-126374800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:126355200-126374800	Weak transcription	HMEC	breast
24	chr8:126355200-126378800	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr8:126355400-126369600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr8:126355600-126369200	Weak transcription	Fetal Muscle Leg	muscle
27	chr8:126355600-126369400	Weak transcription	Adipose Nuclei	Adipose
28	chr8:126355600-126374200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr8:126355600-126374400	Weak transcription	NHLF	lung
30	chr8:126355600-126374600	Weak transcription	NHDF-Ad	bronchial
31	chr8:126355600-126375200	Weak transcription	Small Intestine	intestine
32	chr8:126355800-126369400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr8:126356000-126370800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr8:126356800-126372000	Weak transcription	Liver	Liver
35	chr8:126358000-126369400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr8:126358200-126369200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr8:126358800-126369400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr8:126358800-126376800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr8:126359400-126372200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr8:126359600-126371800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr8:126359800-126369400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:126359800-126369400	Weak transcription	Fetal Lung	lung
43	chr8:126360200-126369000	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr8:126360400-126370200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr8:126360600-126369400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr8:126361400-126369000	Weak transcription	Fetal Muscle Trunk	muscle
47	chr8:126361400-126372000	Weak transcription	Fetal Kidney	kidney
48	chr8:126361600-126369400	Weak transcription	Dnd41	blood
49	chr8:126361800-126371600	Weak transcription	Fetal Intestine Small	intestine
50	chr8:126361800-126372000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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